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Items: 17

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MT-ND1, MT-RNR1
Single nucleotide variant
Mitochondrial disease
+6 more
GPathogenic; drug response
MT-ND1
Single nucleotide variant
Mitochondrial disease
GUncertain significance
MT-ND1
Single nucleotide variant
Mitochondrial disease
GPathogenic
MT-ND1
Single nucleotide variant
Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
GPathogenic
MT-ND1
Single nucleotide variant
Mitochondrial disease
GLikely pathogenic
MT-ND1
Single nucleotide variant
Mitochondrial disease
GLikely pathogenic
MT-ND1
Single nucleotide variant
Mitochondrial disease
GUncertain significance
MT-ND1
Single nucleotide variant
Mitochondrial disease
GUncertain significance
MT-ND1
Single nucleotide variant
Mitochondrial disease
GLikely pathogenic
MT-ND1
Single nucleotide variant
Leigh syndrome
GUncertain significance
MT-ND1
Single nucleotide variant
Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
+2 more
GPathogenic/Likely pathogenic
MT-ND1
Single nucleotide variant
Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
GPathogenic
MT-ND1
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND1
Single nucleotide variant
Leber optic atrophy
GPathogenic
MT-ND1
Single nucleotide variant
Mitochondrial disease
GUncertain significance
MT-ND1
Single nucleotide variant
Leigh syndrome
GBenign
MT-ND4L, MT-ND5
+24 more
Single nucleotide variant
Mitochondrial disease
GPathogenic
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